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  • A MAJOR APPROACH- 2-CHLOROPYRIDINE-5-TRIFLUOROMETHYL DERIVATIVE AS ANTIAMNESIC AGENTS

    About Author:
    Ravindra Singh Tomar
    M.Pharm (Medicinal & Pharmaceutical Chemistry),
    B R Nahta College of Pharmacy, Mandsaur (M.P)
    ravindratomar16@gmail.com

    ABSTRACT-
    Here a scheme has been designed for synthesis of 2-chloropyridine-5-trifluoromethyl derivatives. The probability of being antiamnesic agent has been checked by pass prediction. All compound shows antiamnesic activity as result of pass prediction. By Lipinski rule of five all compounds shows drug like activity. Also a method for pharmacological evaluation & Biochemical evaluation is described under. All synthetic procedure has been designed & described under-

  • THERAPEUTIC POTENTIAL AND FUTURE PROSPECT OF PSIDIUM GUAJAVA LINN

    About Author:
    Aarti Narkhede
    Mahakal Institute of Pharmaceutical Studies,
    Ujjain, MP
    narkhede_aarti@rediffmail.com

    ABSTRACT
    The use of natural product has increased tremendously in a western world as well as in developing countries or in all over part of world. via this artical therapeutic potential and future prospect of Psidium guajava L. are described. Psidium guajava L. belonging to family, myrtaceae. It is a commen tree and easily found in a tropical countries or area. Traditionally it is a very popular and used from long time in a various system of medicine like, unani, Siddha, homeopathy and Ayurveda. It is used for treatment of many ailments like diarrhea, dysentery, wounds, rheumatism, lungs problems, ulcers, skin infections, vaginal discharge, epilepsy, menstrual pain, sore throat, mouth swelling, cold and cough, toothache and etc. In present time study on antipoliferitive or anticancer activities are undertaken and it is found that anticancer activity of P.Guajava has a four time greater than vincristine.

  • A REVIEW: PLANTS AND HERBS USED IN ANXIETY

    About Authors:
    Awan Bharti*1, Sweta Gautam2
    1Department of Pharmacognosy,
    Shri Rawatpura Sarkar Institute of Pharmacy, Datia, M.P.
    2Department of Pharmacognosy, RKDF College of Pharmacy, Bhopal
    *bhartiawan@gmail.com, shwetagautam85@rediffmail

    ABSTRACT
    Interest in alternative medicine and plant-derived medications that affect the "mind" is growing. Anxiety affects one-eighth of the total population of the world and has become a very important area of research interest in psychopharmacology during this decade. Anxiety, a state of excessive fear, is characterized by motor tension, sympathetic hyperactivity, and apprehension and vigilance syndromes. Benzodiazepines are the major class of compounds used in anxiety and they have remained the most commonly prescribed treatment for anxiety, despite the important unwanted side effects that they produce such as sedation, muscle relaxation, ataxia, amnesia, ethanol and barbiturate potentiation and tolerance. Various types of herbal medicines have been used as anxiolytic drugs in different parts of the world. Folk medicines have particular values, for example, plants that "calm down", tranquilize, and raise mood, such as Passiflora coerulea, Valeriana officinalis, Matricaria recutita, Jatropa cilliata, Salvia guaranitica, Tilia tormentosa, and Tilia europeae. Plants have long been used to treat central nervous system (CNS) disorders.

  • “COMPARATIVE ANALYSIS OF VARIOUS PHYSICOCHEMICAL PROPERTIES OF MARKETED PARACETAMOL FORMULATION”

    About Authors:
    Sailesh Narayan*, Ankit Diwan
    Sagar institute of Pharmacy and Technology,
    Gandhi Nagar, Bhopal
    *saileshcology@yahoo.co.in

    INTRODUCTION
    A tablet is a pharmaceutical dosage form. It comprises a mixture of active substances and excipients, usually in powder form, pressed or compacted from  a powder into a solid dose. The excipients can include diluents, binders or granulating agents, glidants and lubricants to ensure efficient tabletting; disintegrants to promote tablet break-up in the digestive tract; sweeteners or flavours to enhance taste; and pigments to make the tablets visually attractive. A polymer coating is often applied to make the tablet smoother and easier to swallow, to control the release rate of the active ingredient, to make it more resistant to the environment or to enhance the tablet's appearance. These are compressed tablets. formulated to deliver an accurate dosage to a specific site; it is usually taken orally, but can be administered sublingually, buccally, rectally or intravaginally. Medicinal tablets were originally made in the shape of a disk of whatever color their components determined, but are now made in many shapes and colors to help distinguish different medicines. Tablets are often stamped with symbols, letters, and numbers, which enable them to be identified.

  • LIQUISOLID COMPACT: A NEW APPROACH TO ENHANCEMENT OF DISSOLUTION OF POORLY WATER SOLUBLE DRUGS

    About Authors:
    Nareshkumar. G1*, A.Eashwar rao2, Ch.Ganga prasad3.
    1*Center for Pharmaceutical Sciences, IST, JNTU Hyderabad, India,
    2Talla Padmavathi College of Pharmacy, Warangal, India,
    3National College of Pharmacy, Shimoga, Karnataka, India.
    *nareshkumar62@gmail.com

    ABSTRACT:
    Liquisolid technique is a new and propitious method that can change the dissolution rate of poorly water soluble drugs. According to the new formulation method of liquisolid compacts, liquid medications such as solutions or suspensions of water insoluble drugs in suitable non-volatile liquid vehicles can be converted into acceptably flowing and compressible powders by blending with selected powder excipients. It has been speculated that such systems exhibit enhanced release profiles. In this case, even though the drug is in a solid dosage form, it is held within the powder substrate in solution or, in a solubilized, almost molecularly dispersed state, which contributes to the enhanced drug dissolution properties. Successful liquisolid tablet is a determination of optimal flowable liquid retention.

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  • A REVIEW OF MITRAGYNA PARVIFOLIA (ROXB) KORTH

    About Authors:
    Sharda roy*, vikas chandra roy, dr. R. C. Roy
    Address Faculty of Pharmaceutical Sciences. Global College of Pharmacy.
    Kahnpur Khui. Punjab.
    *roysharda08@gmail.com

    Abstract:
    Mitragyna parvifolia
    is a medium to large size tree belonging to the family Rubiaceae. It is popularly known as Kaim and is found growing gregariously throughout the drier parts of India, Pakistan and Srilanka. The aerial parts, stem-bark and roots of the tree contain various indolic (tetrahydroalstonine, akkuamigine, hirsuteine etc) and oxindolic (mitraphylline, isomitraphylline, pteropodine, isopteropodine etc) alkaloids. Important variations in the nature and quantity of alkaloids present in different parts of the plant are visible with change in geographical locations. In addition, various parts of the tree such as fruit juice, leaves and stem bark have been used in the traditional system of medicine by the natives and tribal since times immemorial. Mitragyna parvifolia has also got diverse medicinal and therapeutic properties such as analgesic, antipyretic, anti-inflammatory, antiarthritic, anthelmentic, antioxidant etc which have been validated scientifically. In this study we have critically reviewed the pharmacognostic and chemical profile, the traditional and the scientifically validated bioactivities of the plant.

  • NASAL DRUG DELIVERY SYSTEM: A COMPLETE REVIEW

    About Authors:
    Dharmendra Kumar*1, Sumedha Bansal1
    1Department of Pharmaceutical Technology, Meerut Institute of Engineering and Technology,
    Meerut, Uttar Pardesh, India, 250005
    *rvnimiet@gmail.com

    Abstract:
    In present era, nasal drug delivery system has been considered as potential and favourable route of drug delivery because it provides patient compliance, easy to administration, bypass first pass metabolism, excellent penetration, low dose required, rapid absorption and gives desirable effects. So many times nasal drug delivery has been considered as alternative of parenteral route. The purpose of this review, to provide a complete information about nasal drug delivery system such as advantage, limitations, anatomy of nose, mechanism of drug absorption, factors affecting of nasal drug delivery, absorption improvement aspects, novel drug formulations, types of nasal drug delivery system with uses of nasal drug delivery in various disease. So we have expectation, that researches and others cited person get benefitted from this review.

  • A REVIEW ARTICLE ON ANTIFUNGAL AND ANTIMICROBIAL ACTIVITY OF TAGETES ERECTA

    About Author:
    Bandana patel
    Shri Ram Institute Of Technology
    Jabalpur(M.P.) 482002
    Vandanapatel.mbbs@gmail.com

    Abstract:
    Tagetes erectus
    leaf  were evaluated against various gram +ve and gram–ve bacteria and fungi, ethanol extracts exhibited very satisfactory inhibitory activity. Further studies involving the isolation, characterization and purification of the chemical compounds of the plant and screening for antibacterial and antifungal may result in the development of a potent entity which will be of lower toxicity and a high therapeutic value to the mankind.

  • TOTAL PHENOLIC AND FLAVONOID CONTENT OF DIFFERENT EXTRACTS OF INDIGOFERA TINCTORIA LINN

    About Authors:
    Nagasaraswathi.M*, Rafi khan.P, Aleemuddin.MA, Gopi Chand.K, Nagaprashanthi.Ch
    Faculty of Pharmacy, PRIST University,
    Thanjavur-614901, Tamilnadu (INDIA)
    abdulaleemuddin@gmail.com

    ABSTRACT
    The importance for medicinal herbs is increasing day by day due to its high availability and lower side effects. The present study investigated the total phenolic and flavonoid content of various extractions of Indigofera tinctoria linn. The total phenolic content was determined by folin-ciocatechu reagent using Gallic acid as standard and total flavnoid content by aluminium chloride assay using Quercetin as a standard. The present study showed the ratio of phenolic and flavonoid content in different extracts of Indigofera tinctoria linn. Aqueous extract showed the more flavonoid and phenolic content in comparision with other extracts.

  • SYNTHESIS AND BIOLOGICAL EVALUATION OF SOME NOVEL 3-(2-(1H-INDOL-2-YL) PHENYL)-2-ARYLIMIDAZO[4,5-b]INDOLES

    About Authors:
    Aditya Dixit1, Gyanendra Kumar Sharma2, Devender Pathak*3
    1M. Pharmacy (Pharmaceutical Chemistry)
    2Associate Professor (Pharmaceutical chemistry)
    3Director, Professor and Head of the Dept. (Pharmaceutical Chemistry)
    Rajiv Academy for Pharmacy, Mathura,
    Delhi-Mathura Highway, Chhattikara, 281006, India
    dev_15@rediffmail.com*, adixit70@gmail.com

    ABSTRACT
    A traditional but effective method of developing new targets is lead molecule modification, where an existing popular drug from the market is taken as a lead and similar derivatives are synthesized. With the advent of modern techniques conventional methods have lost their gleam but, reactions are still best understood when performed by the conventional techniques. One such endeavor has been made here where indole has been used as a parent moiety and by adding some functional groups some novel indole derivatives were synthesized and screened for their in vitro antitubercular, and anticancer activity. This synthesis of some fresh indole derivatives was done by using various benzaldehyde derivatives and 2-(o-Aminophenyl)indole in acidic condition then with ammonium acetate and isatin in presence of glacial acetic acid.. The structures of newly synthesized compounds were characterized by IR, 1H NMR, MASS and elemental analysis.Compounds 3h & 3i showed good antitubercular activity and 3d, 3e & 3g showed good anticancer compared to the standard drug.

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